| Ident. | Authors (with country if any) | Title |
|---|
| 000115 (2017) |
Ming Zhang [Canada] ; Zhengrui Xi [Canada] ; Karen Misquitta [Canada] ; Christine Sato [Canada] ; Danielle Moreno [Canada] ; Yan Liang [Canada] ; Elizabeth Slow [Canada] ; Ekaterina Rogaeva [Canada] ; Maria Carmela Tartaglia [Canada] | C9orf72 and ATXN2 repeat expansions coexist in a family with ataxia, dementia, and parkinsonism. |
| 000277 (2016) |
Ming Zhang [Canada] ; Zhengrui Xi [Canada] ; Shilun Fang [Canada] ; Mahdi Ghani [Canada] ; Christine Sato [Canada] ; Danielle Moreno [Canada] ; Yan Liang [Canada] ; Anthony E. Lang [Canada] ; Ekaterina Rogaeva [Canada] | Mutation analysis of CHCHD2 in Canadian patients with familial Parkinson's disease. |
| 000669 (2015) |
Zhengrui Xi [Canada] ; Marka Van Blitterswijk [États-Unis] ; Ming Zhang [Canada] ; Philip Mcgoldrick [Canada] ; Jesse R. Mclean [Canada] ; Yana Yunusova [Canada] ; Erin Knock [Canada] ; Danielle Moreno [Canada] ; Christine Sato [Canada] ; Paul M. Mckeever [Canada] ; Raphael Schneider [Canada] ; Julia Keith [Canada] ; Nicolae Petrescu [Canada] ; Paul Fraser [Canada] ; Maria Carmela Tartaglia [Canada] ; Matthew C. Baker [États-Unis] ; Neill R. Graff-Radford [États-Unis] ; Kevin B. Boylan [États-Unis] ; Dennis W. Dickson [États-Unis] ; Ian R. Mackenzie [Canada] ; Rosa Rademakers [États-Unis] ; Janice Robertson [Canada] ; Lorne Zinman [Canada] ; Ekaterina Rogaeva [Canada] | Jump from Pre-mutation to Pathologic Expansion in C9orf72 |
| 000820 (2015) |
Mahdi Ghani ; Christiane Reitz ; Rong Cheng ; Badri Narayan Vardarajan ; Gyungah Jun ; Christine Sato ; Adam Naj ; Ruchita Rajbhandary ; Li-San Wang ; Otto Valladares ; Chiao-Feng Lin ; Eric B. Larson ; Neill R. Graff-Radford ; Denis Evans ; Philip L. De Jager ; Paul K. Crane ; Joseph D. Buxbaum ; Jill R. Murrell ; Towfique Raj ; Nilufer Ertekin-Taner ; Mark Logue ; Clinton T. Baldwin ; Robert C. Green ; Lisa L. Barnes ; Laura B. Cantwell ; M. Daniele Fallin ; Rodney C. P. Go ; Patrick A. Griffith ; Thomas O. Obisesan ; Jennifer J. Manly ; Kathryn L. Lunetta ; M. Ilyas Kamboh ; Oscar L. Lopez ; David A. Bennett ; Hugh Hendrie ; Kathleen S. Hall ; Alison M. Goate ; Goldie S. Byrd ; Walter A. Kukull ; Tatiana M. Foroud ; Jonathan L. Haines ; Lindsay A. Farrer ; Margaret A. Pericak-Vance ; Joseph H. Lee ; Gerard D. Schellenberg ; Peter St. George-Hyslop ; Richard Mayeux ; Ekaterina Rogaeva | Association of Long Runs of Homozygosity With Alzheimer Disease Among African American Individuals |
| 000D72 (2013) |
Zhengrui Xi [Canada] ; Lorne Zinman [Canada] ; Danielle Moreno [Canada] ; Jennifer Schymick [Canada] ; Yan Liang [Canada] ; Christine Sato [Canada] ; Yonglan Zheng [États-Unis] ; Mahdi Ghani [Canada] ; Samar Dib [Canada] ; Julia Keith [Canada] ; Janice Robertson [Canada] ; Ekaterina Rogaeva [Canada] | Hypermethylation of the CpG Island Near the G4C2 Repeat in ALS with a C9orf72 Expansion |
| 000D91 (2013) |
Mahdi Ghani ; Christine Sato ; Joseph H. Lee ; Christiane Reitz ; Danielle Moreno ; Richard Mayeux ; Peter St George-Hyslop ; Ekaterina Rogaeva | Evidence of Recessive Alzheimer Disease Loci in a Caribbean Hispanic Data Set |
| 001221 (2012) |
Zhengrui Xi ; Lorne Zinman ; Yakov Grinberg ; Danielle Moreno ; Christine Sato ; Juan M. Bilbao ; Mahdi Ghani ; Isabel Hernández ; Agustín Ruiz ; Mercè Boada ; Francisco J. Mor N ; Anthony E. Lang ; Connie Marras ; Amalia Bruni ; Rosanna Colao ; Raffaele G. Maletta ; Gianfranco Puccio ; Innocenzo Rainero ; Lorenzo Pinessi ; Daniela Galimberti ; Karen E. Morrison ; Catriona Moorby ; Joanne D. Stockton ; Mario Masellis ; Sandra E. Black ; Lili-Naz Hazrati ; Yan Liang ; Jan Van Haersma De With ; Luis Fornazzari ; Roque Villagra ; Ricardo Rojas-Garcia ; Jordi Clarim N ; Richard Mayeux ; Janice Robertson ; Peter St George-Hyslop ; Ekaterina Rogaeva | Investigation of C9orf72 in 4 Neurodegenerative Disorders |
| 001560 (2012) |
ZHENGRUI XI [Canada] ; Lome Zinman [Canada] ; Yakov Grinberg [Canada] ; Danielle Moreno ; Christine Sato [Canada] ; Juan M. Bilbao [Canada] ; Mahdi Ghani [Canada] ; Isabel Hernandez [Espagne] ; Agustín Ruiz [Espagne] ; Mercè Boada [Espagne] ; Francisco J. Moron [Canada, Espagne] ; Anthony E. Lang [Canada] ; Connie Marras [Canada] ; Amalia Bruni [Italie] ; Rosanna Colao [Italie] ; Raffaele G. Maletta [Italie] ; Gianfranco Puccio [Italie] ; Innocenzo Rainero [Italie] ; Lorenzo Pinessi [Italie] ; Daniela Galimberti [Italie] ; Karen E. Morrison [États-Unis] ; Catriona Moorby [États-Unis] ; Joanne D. Stockton [États-Unis] ; Mario Masellis [Canada] ; Sandra E. Black [Canada] ; Lili-Naz Hazrati [Canada] ; YAN LIANG [Canada] ; Jan Van Haersma De With [Canada] ; Luis Fornazzari [Canada] ; Roque Villagra [Chili] ; Ricardo Rojas-Garcia [Canada, Espagne] ; Jordi Clarimon [Espagne] ; Richard Mayeux [États-Unis] ; Janice Robertson [Canada] ; Peter St George-Hyslop [Canada, Royaume-Uni] ; Ekaterina Rogaeva [Canada] | Investigation of C9orf72 in 4 Neurodegenerative Disorders |
| 001E21 (2010) |
Connie Marras [Canada] ; Christine Klein [Canada, Allemagne] ; Anthony E. Lang [Canada] ; Yosuke Wakutani [Canada] ; Danielle Moreno [Canada] ; Christine Sato [Canada] ; Edwin Yip [Canada] ; Renato P. Munhoz [Brésil] ; Katja Lohmann [Allemagne] ; Ana Dj Armati [Allemagne] ; Andrew Bi [Canada] ; Ekaterina Rogaeva [Canada] | LRRK2 and Parkin mutations in a family with parkinsonism-Lack of genotype-phenotype correlation |
| 002456 (2008) |
Renato P. Munhoz [Brésil] ; Yosuke Wakutani [Canada] ; Connie Marras [Canada] ; Helio A. Teive [Brésil] ; Salmo Raskin [Brésil] ; Lineu C. Werneck [Brésil] ; Danielle Moreno [Canada] ; Christine Sato [Canada] ; Anthony E. Lang [Canada] ; Ekaterina Rogaeva [Canada] | The G2019S LRRK2 mutation in Brazilian patients with Parkinson's disease: Phenotype in monozygotic twins |
| 002569 (2008) |
Renato P. Munhoz [Brésil] ; Yosuke Wakutani [Canada] ; Connie Marras [Canada] ; Helio A. Teive [Brésil] ; Salmo Raskin [Brésil] ; Lineu C. Werneck [Brésil] ; Danielle Moreno [Canada] ; Christine Sato [Canada] ; Anthony E. Lang [Canada] ; Ekaterina Rogaeva [Canada] | The G2019S LRRK2 Mutation in Brazilian Patients with Parkinson's Disease : Phenotype in Monozygotic Twins |
| 002A54 (2006) |
Cindy Zadikoff [Canada] ; Ekaterina Rogaeva [Canada] ; Ana Djarmati [Allemagne] ; Christine Sato [Canada] ; Shabnam Salehi-Rad [Canada] ; Peter St. George-Hyslop [Canada] ; Christine Klein [Canada, Allemagne] ; Anthony E. Lang [Canada] | Homozygous and heterozygous PINK1 mutations: Considerations for diagnosis and care of Parkinson's disease patients |
| 002A60 (2006) |
Mario Masellis [Canada] ; Parastoo Momeni [États-Unis, Canada] ; Wendy Meschino [Canada] ; Reid Heffner [États-Unis, Canada] ; Joshua Elder [États-Unis, Canada] ; Christine Sato [Canada] ; Yan Liang [Canada] ; Peter St George-Hyslop [Canada] ; John Hardy [États-Unis, Canada] ; Juan Bilbao [Canada] ; Sandra Black [Canada] ; Ekaterina Rogaeva [Canada] | Novel splicing mutation in the progranulin gene causing familial corticobasal syndrome |
| 002B06 (2006) |
Satoshi Kaneko [Japon] ; Toshitaka Kawarai [Canada] ; Edwin Yip [Canada] ; Shabnam Salehi-Rad [Canada] ; Christine Sato [Canada] ; Antonio Orlacchio [Italie] ; Giorgio Bernardi [Italie] ; Yan Liang [Canada] ; Hiroshi Hasegawa [Canada] ; Ekaterina Rogaeva [Canada] ; Peter St George-Hyslop [Canada] | Novel SPG6 mutation p.A100T in a Japanese family with autosomal dominant form of hereditary spastic paraplegia |
| 002B53 (2006) |
Renato P. Munhoz [Brésil] ; Toshitaka Kawarai [Canada] ; Helio A. Teive [Brésil] ; Salmo Raskin [Brésil] ; Christine Sato [Canada] ; Yan Liang [Canada] ; Peter H. St. George-Hyslop [Canada] ; Ekaterina Rogaeva [Canada] | Clinical and genetic study of a Brazilian family with spastic paraplegia (SPG6 locus) |
| 002B89 (2006) |
Muhammad A. Chishti [Arabie saoudite] ; Saeed Bohlega [Arabie saoudite] ; Maqbool Ahmed [Arabie saoudite] ; Arslan Loualich [Arabie saoudite] ; Pamela Carroll [Arabie saoudite] ; Christine Sato [Canada] ; Peter St George-Hyslop [Canada] ; David Westaway [Canada] ; Ekaterina Rogaeva [Canada] | T313M PINK1 mutation in an extended highly consanguineous saudi family with early-onset parkinson disease |
| 002C21 (2006) |
Cindy Zadikoff [Canada] ; Ekaterina Rogaeva [Canada] ; Ana Djarmati [Allemagne] ; Christine Sato [Canada] ; Shabnam Salehi-Rad [Canada] ; Peter St. George-Hyslop [Canada] ; Christine Klein [Canada, Allemagne] ; Anthony E. Lang [Canada] | Homozygous and heterozygous PINK1 mutations : Considerations for diagnosis and care of parkinson's disease patients |
| 002E15 (2005) |
Christine Sato [Canada] ; Angharad Morgan [Canada] ; Anthony E. Lang [Canada] ; Shabnam Salehi-Rad [Canada] ; Toshitaka Kawarai [Canada] ; Yan Meng [États-Unis] ; Peter N. Ray [Canada] ; Lindsay A. Farrer [États-Unis] ; Peter St George-Hyslop [Canada] ; Ekaterina Rogaeva [Canada] | Analysis of the glucocerebrosidase gene in Parkinson's disease |
| 002F35 (2004) |
Justus L. Groen [Canada] ; Toshitaka Kawarai ; Anna Toulina ; Chiara Rivoiro ; Shabnam Salehi-Rad ; Christine Sato ; Angharad Morgan ; Yan Liang ; Ronald B. Postuma ; Peter St George-Hyslop ; Anthony E. Lang ; Ekaterina Rogaeva | Genetic association study of PINK1 coding polymorphisms in Parkinson's disease. |
| 002F58 (2004) |
Ekaterina Rogaeva [Canada] ; Janel Johnson ; Anthony E. Lang ; Cindy Gulick ; Katrina Gwinn-Hardy ; Toshitaka Kawarai ; Christine Sato ; Angharad Morgan ; John Werner ; Robert Nussbaum ; Agnes Petit ; Michael S. Okun ; Aideen Mcinerney ; Ronald Mandel ; Justus L. Groen ; Hubert H. Fernandez ; Ron Postuma ; Kelly D. Foote ; Shabnam Salehi-Rad ; Yan Liang ; Sharon Reimsnider ; Anurag Tandon ; John Hardy ; Peter St George-Hyslop ; Andrew B. Singleton | Analysis of the PINK1 gene in a large cohort of cases with Parkinson disease. |
| 003100 (2004) |
Justus L. Groen [Canada] ; Toshitaka Kawarai [Canada] ; Anna Toulina [Canada] ; Chiara Rivoiro [Canada, Italie] ; Shabnam Salehi-Rad [Canada] ; Christine Sato [Canada] ; Angharad Morgan [Canada] ; YAN LIANG [Canada] ; Ronald B. Postuma [Canada] ; Peter St George-Hyslop [Canada] ; Anthony E. Lang [Canada] ; Ekaterina Rogaeva [Canada] | Genetic association study of PINK1 coding polymorphisms in Parkinson's disease |
